检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:胡跃强[1] 唐农[2] 吴林[2] 孙淑荣[1] 苏锦勋[2] 覃琴[1]
机构地区:[1]广西中医药大学第一附属医院神经内科,南宁530023 [2]广西中医药大学
出 处:《中华老年心脑血管病杂志》2013年第12期1321-1323,共3页Chinese Journal of Geriatric Heart,Brain and Vessel Diseases
基 金:广西自然科学基金(2012GXNSFAA053075);广西卫生厅重点课题(2012046)
摘 要:目的观察脑缺血后处理中,联合水蛭注射液进行后处理,对脑缺血损伤大鼠磷酸化蛋白激酶B mRNA及其蛋白表达的影响。方法 SD大鼠40只,随机分为假手术组(SO组)、缺血再灌注组(I/R组)、缺血后处理组(IPOC组)、IPOC+水蛭注射液后处理组(P-L组),每组10只。采用线栓法制备大鼠大脑中动脉闭塞模型及IPOC模型,应用实时荧光定量PCR和Western blot法检测磷酸化蛋白激酶mRNA及其蛋白表达。结果 SO组有少量磷酸化蛋白激酶mRNA及蛋白表达;与SO组比较,I/R组表达明显升高;与I/R组比较,IPOC组表达明显升高(P<0.01);与IPOC组比较,P-L组表达明显升高(P<0.05)。结论 IPOC可能通过诱导磷酸化蛋白激酶的表达发挥其神经保护作用,水蛭注射液可进一步促进其表达而发挥神经保护作用。Objective To study the effect of combined leech injection and ischemic postconditioning on expression of p-Akt mRNA and protein in rats following I/R injury. Methods Forty male SD rats were randomly divided into sham operation group, I/R group, ischemie posteonditioning group and leech injection postconditioning group (10 in each group). A middle cerebral artery oc- clusion model and an isehemie posteonditioning model were established by Longa occlusion. Ex- pression of p-Akt mRNA and protein was detected by RT-PCR and Western blot, respectively. Results Only a mall amount of p-Akt mRNA and protein was expressed in sham operation group. The expression level of p-Akt mRNA and protein was significantly higher in I/R group than in sham operation group,in ischemie postconditioning group than in I/R group, and in leech injection postconditioning group than in ischemie postconditioning group (P〈0.05). Conclusion Ischemic posteonditioning can protect nerves by inducing p-Akt expression and leech injection postconditioning plays an important role in protection of nerves by further promoting its expression.
关 键 词:药用水蛭 脑缺血 蛋白激酶类 再灌注损伤 RNA 信使
分 类 号:R743[医药卫生—神经病学与精神病学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.120